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SCLC-CellMiner: A Resource for Small Cell Lung Cancer Cell Line Genomics and Pharmacology Based on Genomic Signatures
CellMiner-SCLC (https://discover.nci.nih.gov/SclcCellMinerCDB/) integrates drug sensitivity and genomic data, including high-resolution methylome and transcriptome from 118 patient-derived small cell lung cancer (SCLC) cell lines, providing a resource for research into this “recalcitrant cancer.” We...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643325/ https://www.ncbi.nlm.nih.gov/pubmed/33086069 http://dx.doi.org/10.1016/j.celrep.2020.108296 |
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author | Tlemsani, Camille Pongor, Lorinc Elloumi, Fathi Girard, Luc Huffman, Kenneth E. Roper, Nitin Varma, Sudhir Luna, Augustin Rajapakse, Vinodh N. Sebastian, Robin Kohn, Kurt W. Krushkal, Julia Aladjem, Mirit I. Teicher, Beverly A. Meltzer, Paul S. Reinhold, William C. Minna, John D. Thomas, Anish Pommier, Yves |
author_facet | Tlemsani, Camille Pongor, Lorinc Elloumi, Fathi Girard, Luc Huffman, Kenneth E. Roper, Nitin Varma, Sudhir Luna, Augustin Rajapakse, Vinodh N. Sebastian, Robin Kohn, Kurt W. Krushkal, Julia Aladjem, Mirit I. Teicher, Beverly A. Meltzer, Paul S. Reinhold, William C. Minna, John D. Thomas, Anish Pommier, Yves |
author_sort | Tlemsani, Camille |
collection | PubMed |
description | CellMiner-SCLC (https://discover.nci.nih.gov/SclcCellMinerCDB/) integrates drug sensitivity and genomic data, including high-resolution methylome and transcriptome from 118 patient-derived small cell lung cancer (SCLC) cell lines, providing a resource for research into this “recalcitrant cancer.” We demonstrate the reproducibility and stability of data from multiple sources and validate the SCLC consensus nomenclature on the basis of expression of master transcription factors NEUROD1, ASCL1, POU2F3, and YAP1. Our analyses reveal transcription networks linking SCLC subtypes with MYC and its paralogs and the NOTCH and HIPPO pathways. SCLC subsets express specific surface markers, providing potential opportunities for antibody-based targeted therapies. YAP1-driven SCLCs are notable for differential expression of the NOTCH pathway, epithelial-mesenchymal transition (EMT), and antigen-presenting machinery (APM) genes and sensitivity to mTOR and AKT inhibitors. These analyses provide insights into SCLC biology and a framework for future investigations into subtype-specific SCLC vulnerabilities. |
format | Online Article Text |
id | pubmed-7643325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-76433252020-11-05 SCLC-CellMiner: A Resource for Small Cell Lung Cancer Cell Line Genomics and Pharmacology Based on Genomic Signatures Tlemsani, Camille Pongor, Lorinc Elloumi, Fathi Girard, Luc Huffman, Kenneth E. Roper, Nitin Varma, Sudhir Luna, Augustin Rajapakse, Vinodh N. Sebastian, Robin Kohn, Kurt W. Krushkal, Julia Aladjem, Mirit I. Teicher, Beverly A. Meltzer, Paul S. Reinhold, William C. Minna, John D. Thomas, Anish Pommier, Yves Cell Rep Article CellMiner-SCLC (https://discover.nci.nih.gov/SclcCellMinerCDB/) integrates drug sensitivity and genomic data, including high-resolution methylome and transcriptome from 118 patient-derived small cell lung cancer (SCLC) cell lines, providing a resource for research into this “recalcitrant cancer.” We demonstrate the reproducibility and stability of data from multiple sources and validate the SCLC consensus nomenclature on the basis of expression of master transcription factors NEUROD1, ASCL1, POU2F3, and YAP1. Our analyses reveal transcription networks linking SCLC subtypes with MYC and its paralogs and the NOTCH and HIPPO pathways. SCLC subsets express specific surface markers, providing potential opportunities for antibody-based targeted therapies. YAP1-driven SCLCs are notable for differential expression of the NOTCH pathway, epithelial-mesenchymal transition (EMT), and antigen-presenting machinery (APM) genes and sensitivity to mTOR and AKT inhibitors. These analyses provide insights into SCLC biology and a framework for future investigations into subtype-specific SCLC vulnerabilities. 2020-10-20 /pmc/articles/PMC7643325/ /pubmed/33086069 http://dx.doi.org/10.1016/j.celrep.2020.108296 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Tlemsani, Camille Pongor, Lorinc Elloumi, Fathi Girard, Luc Huffman, Kenneth E. Roper, Nitin Varma, Sudhir Luna, Augustin Rajapakse, Vinodh N. Sebastian, Robin Kohn, Kurt W. Krushkal, Julia Aladjem, Mirit I. Teicher, Beverly A. Meltzer, Paul S. Reinhold, William C. Minna, John D. Thomas, Anish Pommier, Yves SCLC-CellMiner: A Resource for Small Cell Lung Cancer Cell Line Genomics and Pharmacology Based on Genomic Signatures |
title | SCLC-CellMiner: A Resource for Small Cell Lung Cancer Cell Line Genomics and Pharmacology Based on Genomic Signatures |
title_full | SCLC-CellMiner: A Resource for Small Cell Lung Cancer Cell Line Genomics and Pharmacology Based on Genomic Signatures |
title_fullStr | SCLC-CellMiner: A Resource for Small Cell Lung Cancer Cell Line Genomics and Pharmacology Based on Genomic Signatures |
title_full_unstemmed | SCLC-CellMiner: A Resource for Small Cell Lung Cancer Cell Line Genomics and Pharmacology Based on Genomic Signatures |
title_short | SCLC-CellMiner: A Resource for Small Cell Lung Cancer Cell Line Genomics and Pharmacology Based on Genomic Signatures |
title_sort | sclc-cellminer: a resource for small cell lung cancer cell line genomics and pharmacology based on genomic signatures |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643325/ https://www.ncbi.nlm.nih.gov/pubmed/33086069 http://dx.doi.org/10.1016/j.celrep.2020.108296 |
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